Adecco Lifesciences are working with a long-standing and highly successful Medical Device manufacturer who is looking for a Graduate/Entry Level Regulatory Associate to join the team on a permanent basis.
The existing team is already strong and so you will work alongside motivated and experienced RA Specialists, learning as you go, supporting the company with Technical File remediation for existing products to ensure compliance to MDR (2017/745) and assist in the creation of technical documentation for new products being introduced in the New Year.
Day to day you can expect to:
Create and maintain Technical Files in accordance with EC Regulation 93/42/EEC.
Transition Technical Files from Medical Devices Directive (93/42/EEC) to Medical Devices Regulation (2017/745)
Compile Technical Files and documentation for review by the Notified Body.
Provide regulatory support for all post-market surveillance activities.
Maintain and approve product labeling to meet regulatory & UDI requirements.
If you are adaptable, productive and can work well in a team, you will thrive in this position.
As this is an entry-level role, the client are looking for a person to have a desire to work with a Medical Device business and a passion to learn Regulatory Affairs, alongside a degree in Life Sciences.
The business strives to offer each candidate continuous professional development and education allowing you to gain further knowledge in the regulatory field.
If this role is of interest and you have the relevant experience, then please apply and I will be in touch to talk in more detail.
To speak to a recruitment expert please contact Amy Holder